A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3184



Internal ID15537912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99173824..99193714hg38UCSC Ensembl
Outerchr3:98892668..98912558hg19UCSC Ensembl
Outerchr3:100375358..100395248hg18UCSC Ensembl
Outerchr3:100375358..100395248hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3819891
hg1919891
hg1819891
hg1719891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3915
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3184
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer